@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_head
{
this:
np:hasAssertion
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_assertion
;
np:hasProvenance
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_provenance
;
np:hasPublicationInfo
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_assertion
a
np:Assertion
.
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_provenance
a
np:Provenance
.
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0679466
a
ncit:C7057
.
dgn-gda:DGN902363ff712c6c6346d218a4c27e14c8
sio:SIO_000628
miriam-gene:351
,
lld:C0679466
;
a
sio:SIO_001121
.
}
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_provenance
{
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_assertion
dcterms:description
"[This interpretation of one aspect of the cognitive deficit in human mutant APP mice has parallels to deficits observed in patients with Alzheimer's disease, further supporting the validity of transgenic models of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:18772249
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP339866.RAlrphk9PksFoYFHihasCyk9MEGnup4dU0OtzyylyfTXw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:20+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}